NDC 15631-0220

HELLEBORUS FOETIDUS

Helleborus Foetidus

HELLEBORUS FOETIDUS is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Rxhomeo Private Limited D.b.a. Rxhomeo, Inc. The primary component is Helleborus Foetidus Root.

Product ID15631-0220_a1470309-036c-1159-e053-2a95a90ab0b0
NDC15631-0220
Product TypeHuman Otc Drug
Proprietary NameHELLEBORUS FOETIDUS
Generic NameHelleborus Foetidus
Dosage FormPellet
Route of AdministrationORAL
Marketing Start Date2015-10-31
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameRxhomeo Private Limited d.b.a. Rxhomeo, Inc
Substance NameHELLEBORUS FOETIDUS ROOT
Active Ingredient Strength3 [hp_X]/1
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 15631-0220-0

100 PELLET in 1 PACKAGE (15631-0220-0)
Marketing Start Date2018-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 15631-0220-0 [15631022000]

HELLEBORUS FOETIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0220-3 [15631022003]

HELLEBORUS FOETIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0220-1 [15631022001]

HELLEBORUS FOETIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0220-4 [15631022004]

HELLEBORUS FOETIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0220-5 [15631022005]

HELLEBORUS FOETIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

NDC 15631-0220-2 [15631022002]

HELLEBORUS FOETIDUS PELLET
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-01-01
Inactivation Date2020-01-31
Reactivation Date2020-03-20

Drug Details

Active Ingredients

IngredientStrength
HELLEBORUS FOETIDUS ROOT3 [hp_X]/1

OpenFDA Data

SPL SET ID:5543a329-625e-4efd-8389-3f0981d02a15
Manufacturer
UNII

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.